Association of the Hepatocyte Growth Factor Gene with Keratoconus in an Australian Population

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

(2013) Yi Lu et al.   NATURE GENETICS

Proteases, proteolysis and inflammatory molecules in the tears of people with keratoconus

(2012) Sivaraman Arumugam Balasubramanian et al.   ACTA OPHTHALMOLOGICA

Collagen cross-linking: a new treatment paradigm in corneal disease - a review

(2010) Grant R Snibson   CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

Absence of Pathogenic Mutations in VSX1 and SOD1 Genes in Patients With Keratoconus

(2010) Mirna Štabuc-Šilih et al.   CORNEA

The GEnes in Myopia (GEM) study in understanding the aetiology of refractive errors

(2010) Paul N. Baird et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Subclinical keratoconus and inflammatory molecules from tears

(2009) I Lema et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Three VSX1 Gene Mutations, L159M, R166W, and H244R, Are Not Associated With Keratoconus

(2009) Yongming G Tang et al.   CORNEA

Mutational screening of VSX1 in keratoconus patients from the European population

(2009) D P Dash et al.   EYE

Role of the Hepatocyte Growth Factor Gene in Refractive Error

(2009) Sundar Veerappan et al.   OPHTHALMOLOGY

VSX1 gene variants are associated with keratoconus in unrelated Korean patients

(2008) Jee-Won Mok et al.   JOURNAL OF HUMAN GENETICS

The D144E Substitution in theVSX1Gene: A Non-pathogenic Variant or a Disease Causing Mutation?

(2008) Pras Eran et al.   OPHTHALMIC GENETICS